Kelly W.N.,1983

Kelly W.N., Wyngaarden J.B. Clinical syndromes associated with human hypoxanthine-guanine phosphoribosyltransferase deficiency. - The Metabolic Basis of Inherited Disease. - Ed. Stanbury J.B., Wyngaarden J.B., Fredrickson D.S., Goldstein J.L., Brown M.S., 1983, p. 1115-1144.

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